IS1999B - 4-Aryl-1-phenylalkyl-1,2,3,6-tetrahydropyridine having neuromuscular and neurotransmitter activity - Google Patents

4-Aryl-1-phenylalkyl-1,2,3,6-tetrahydropyridine having neuromuscular and neurotransmitter activity

Info

Publication number
IS1999B
IS1999B IS4641A IS4641A IS1999B IS 1999 B IS1999 B IS 1999B IS 4641 A IS4641 A IS 4641A IS 4641 A IS4641 A IS 4641A IS 1999 B IS1999 B IS 1999B
Authority
IS
Iceland
Prior art keywords
alkyl
tetrahydropyridine
aryl
phenylalkyl
neuromuscular
Prior art date
Application number
IS4641A
Other languages
Icelandic (is)
Other versions
IS4641A (en
Inventor
Badone Domenico
Baroni Marco
Cardamone Rosanna
Fournier Jacqueline
Guzzi Umberto
Ielmini Alessandra
Original Assignee
Sanofi-Aventis
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sanofi-Aventis filed Critical Sanofi-Aventis
Publication of IS4641A publication Critical patent/IS4641A/en
Publication of IS1999B publication Critical patent/IS1999B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40Oxygen atoms
    • C07D211/44Oxygen atoms attached in position 4
    • C07D211/52Oxygen atoms attached in position 4 having an aryl radical as the second substituent in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/70Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)

Abstract

4-Aryl-1-phenyl alkyl-1,2,3,6-tetrahydropyridine derivs. of formula (I), their salts, solvates and quat. ammonium salts are new. Y = CH or N; R1 = H, halo, CF3, 3-4C alkyl or 1-4C alkoxy; R2 = as R1 or OH; R3, R4 = H or 1-3C alkyl; X = 3-6C alkyl, 3-6C alkoxy, 3-7C carboxyalkyl, (1-4C) alkoxycarbonyl(3-6C)alkyl, 3-7C carboxyalkoxy or (1-4C)alkoxycarbonyl(3-6C)alkoxy; or 3-7C cycloalkyl, 3-7C cycloalkoxy, (3-7C)cycloalkylmethyl, 3-7C cycloalkylamino or cyclohexenyl (all opt. substd.); or phenyl, phenoxy, phenylamino, N-(1-3C)alkylphenylamino, phenylmethyl, phenylethyl, phenylcarbonyl, phenylthio, phenylsulphonyl, phenylsulphinyl or styryl (all opt. substd.)
IS4641A 1995-06-28 1997-12-23 4-Aryl-1-phenylalkyl-1,2,3,6-tetrahydropyridine having neuromuscular and neurotransmitter activity IS1999B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9507760A FR2736053B1 (en) 1995-06-28 1995-06-28 NEWS 1-PHENYLALKYL-1,2,3,6-TETRAHYDROPYRIDINES
PCT/FR1996/000995 WO1997001536A1 (en) 1995-06-28 1996-06-26 4-aryl-1-phenylalkyl-1,2,3,6-tetrahydropyridines having neurotrophic and neuroprotective activity

Publications (2)

Publication Number Publication Date
IS4641A IS4641A (en) 1997-12-23
IS1999B true IS1999B (en) 2005-04-15

Family

ID=9480466

Family Applications (1)

Application Number Title Priority Date Filing Date
IS4641A IS1999B (en) 1995-06-28 1997-12-23 4-Aryl-1-phenylalkyl-1,2,3,6-tetrahydropyridine having neuromuscular and neurotransmitter activity

Country Status (30)

Country Link
US (1) US5981754A (en)
EP (2) EP1216996A3 (en)
JP (2) JP3147906B2 (en)
KR (1) KR100460581B1 (en)
CN (1) CN1153765C (en)
AT (1) ATE223897T1 (en)
AU (1) AU715090B2 (en)
BR (1) BR9608662A (en)
CA (1) CA2225746C (en)
CY (1) CY2312B1 (en)
CZ (1) CZ291075B6 (en)
DE (1) DE69623631T2 (en)
DK (1) DK0837848T3 (en)
EE (1) EE03870B1 (en)
ES (1) ES2183965T3 (en)
FR (1) FR2736053B1 (en)
HK (1) HK1014952A1 (en)
HU (1) HUP9900055A3 (en)
IL (1) IL122159A (en)
IS (1) IS1999B (en)
NO (1) NO310144B1 (en)
NZ (1) NZ312723A (en)
PL (2) PL187087B1 (en)
PT (1) PT837848E (en)
RU (1) RU2163237C2 (en)
SK (2) SK285433B6 (en)
TR (1) TR199701710T1 (en)
UA (1) UA62914C2 (en)
WO (1) WO1997001536A1 (en)
ZA (1) ZA965527B (en)

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FR2762514B1 (en) 1997-04-29 1999-10-22 Sanofi Sa USE OF TETRAHYDROPYRIDINE DERIVATIVES FOR THE PREPARATION OF MEDICINES FOR THE TREATMENT OF DISEASES LEADING TO DEMYELINATION
FR2763847B1 (en) * 1997-05-28 2003-06-06 Sanofi Sa USE OF 4-SUBSTITUTED TETRAHYDROPYRIDINES FOR MANUFACTURING TGF-BETA-1 MEDICAMENTS
FR2771006B1 (en) * 1997-11-14 2000-12-01 Sanofi Sa COMBINATION OF ACTIVE INGREDIENTS FOR THE TREATMENT OF SENILE DEMENTIA OF THE ALZHEIMER TYPE
FR2771007B1 (en) * 1997-11-14 2000-12-01 Sanofi Sa COMBINATION OF ACTIVE INGREDIENTS FOR THE TREATMENT OF SENILE DEMENTIA OF THE ALZHEIMER TYPE
CO4980891A1 (en) * 1997-11-14 2000-11-27 Sanofi Sa ASSOCIATION OF ACTIVE PRINCIPLES FOR THE TREATMENT OF SENILE DEMENTIA OF THE AZHEIMER TYPE
JP2002518386A (en) * 1998-06-19 2002-06-25 イーライ・リリー・アンド・カンパニー Production of heteroaryl compounds
FR2803593B1 (en) * 2000-01-06 2002-02-15 Sanofi Synthelabo NOVEL TETRAHYDROPYRIDINES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
FR2823748B1 (en) * 2001-04-20 2004-02-20 Sanofi Synthelabo TETRAHYDROPYRIDYL-ALKYL-BENZODIAZINES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
WO2002085888A1 (en) * 2001-04-20 2002-10-31 Sanofi-Synthelabo Tetrahydropyridyl-alkyl-heterocycles, method for preparing same and pharmaceutical compositions containing same
FR2840896B1 (en) * 2002-06-18 2005-04-08 Sanofi Synthelabo PHENYL AND PYRIDYL PIPERAZINES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
BR0316785A (en) * 2002-12-16 2005-10-25 Mitsubishi Pharma Corp 4-Pyrimidone-3-substituted derivatives
JP4866610B2 (en) 2003-08-18 2012-02-01 富士フイルムファインケミカルズ株式会社 Pyridyltetrahydropyridines and pyridylpiperidines
TWI350168B (en) * 2004-05-07 2011-10-11 Incyte Corp Amido compounds and their use as pharmaceuticals
EA200700117A1 (en) * 2004-06-24 2007-06-29 Инсайт Корпорейшн N-SUBSTITUTED PIPERIDINES AND THEIR APPLICATION AS PHARMACEUTICAL PREPARATIONS
US20060009491A1 (en) * 2004-06-24 2006-01-12 Incyte Corporation Amido compounds and their use as pharmaceuticals
JP2008504274A (en) * 2004-06-24 2008-02-14 インサイト・コーポレイション Amide compounds and their use as pharmaceuticals
JP2008504280A (en) 2004-06-24 2008-02-14 インサイト・コーポレイション 2-methylpropanamide and its pharmaceutical use
MXPA06014572A (en) * 2004-06-24 2007-03-12 Incyte Corp Amido compounds and their use as pharmaceuticals.
KR20070050076A (en) * 2004-08-10 2007-05-14 인사이트 산 디에고 인코포레이티드 Amido compounds and their use as pharmaceuticals
GEP20125565B (en) * 2004-11-10 2012-07-10 Incyte Corp Lactam compounds and their pharmaceutical use
US8110581B2 (en) * 2004-11-10 2012-02-07 Incyte Corporation Lactam compounds and their use as pharmaceuticals
BRPI0518281A2 (en) * 2004-11-18 2008-11-18 Incyte Corp 11-beta hydroxylesterase dehydrogenase type i inhibitors and methods of using them
FR2883285B1 (en) * 2005-03-17 2007-05-18 Sanofi Aventis Sa 7- (2- (4- (3-TRIFLUOROMETHYL-PHENYL) -1,2,3,6-TETRAHUDRO-PYRID-1-YL) ETHYL) ISOQUINOLINE BESYLATE SALT, ITS PREPARATION AND USE IN THERAPEUTICS
JP4864342B2 (en) * 2005-04-27 2012-02-01 北興化学工業株式会社 Method for producing biaryl compound
JP2009508963A (en) * 2005-09-21 2009-03-05 インサイト・コーポレイション Amide compounds and their use as pharmaceutical compositions
CA2630492C (en) * 2005-12-05 2015-04-14 Incyte Corporation Spiro-lactam compounds
WO2007084314A2 (en) * 2006-01-12 2007-07-26 Incyte Corporation MODULATORS OF 11-ß HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME
KR20080091503A (en) * 2006-01-31 2008-10-13 인사이트 코포레이션 Amido compounds and their use as pharmaceuticals
US20070213311A1 (en) * 2006-03-02 2007-09-13 Yun-Long Li Modulators of 11-beta hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same
WO2007103719A2 (en) * 2006-03-03 2007-09-13 Incyte Corporation MODULATORS OF 11-β HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME
JP2009535420A (en) * 2006-05-01 2009-10-01 インサイト・コーポレイション Tetra-substituted ureas as modulators of 11-beta hydroxyl steroid dehydrogenase type 1
US7838544B2 (en) * 2006-05-17 2010-11-23 Incyte Corporation Heterocyclic inhibitors of 11-β hydroxyl steroid dehydrogenase type 1 and methods of using the same
CL2008001839A1 (en) 2007-06-21 2009-01-16 Incyte Holdings Corp Compounds derived from 2,7-diazaspirocycles, inhibitors of 11-beta hydroxyl steroid dehydrogenase type 1; pharmaceutical composition comprising said compounds; Useful to treat obesity, diabetes, glucose intolerance, type II diabetes, among other diseases.
KR20100135711A (en) 2007-12-20 2010-12-27 엔비보 파마슈티칼즈, 인코퍼레이티드 Tetrasubstituted benzenes
WO2011089072A1 (en) * 2010-01-19 2011-07-28 Bayer Cropscience Ag Method for producing aryl and heteroarylacetic acid derivatives
WO2018195649A1 (en) * 2017-04-26 2018-11-01 Alberta Research Chemicals Inc. Substituted tetrahydropyridine derivatives as ido-1 inhibitors and uses thereof

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EP0398578B1 (en) * 1989-05-17 1997-03-12 Pfizer Inc. 2-piperidino-1-alkanol derivatives as antiischemic agents
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FR2662355B1 (en) * 1990-05-22 1994-11-10 Sanofi Sa USE OF 1- [2- (2-NAPHTYL) ETHYL] -4- (3-TRIFLUOROMETHYLPHENYL) -1,2,3,6-TETRAHYDROPYRIDINE FOR THE PREPARATION OF MEDICINES FOR THE TREATMENT OF BRAIN AND NEURAL DISORDERS.
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DE4325855A1 (en) * 1993-08-02 1995-02-09 Boehringer Ingelheim Kg Novel benzoic acid derivatives, processes for their preparation and their use as medicaments

Also Published As

Publication number Publication date
EE03870B1 (en) 2002-10-15
SK178197A3 (en) 1998-07-08
EP0837848A1 (en) 1998-04-29
AU6461996A (en) 1997-01-30
CZ291075B6 (en) 2002-12-11
PL187087B1 (en) 2004-05-31
PT837848E (en) 2002-12-31
IL122159A0 (en) 1998-04-05
FR2736053B1 (en) 1997-09-19
NO976079L (en) 1997-12-23
ATE223897T1 (en) 2002-09-15
EP1216996A2 (en) 2002-06-26
EP1216996A3 (en) 2003-10-15
DE69623631T2 (en) 2003-08-07
EE9700348A (en) 1998-06-15
ES2183965T3 (en) 2003-04-01
BR9608662A (en) 1999-05-04
TR199701710T1 (en) 1998-05-21
JP2001114763A (en) 2001-04-24
SK285433B6 (en) 2007-01-04
NO976079D0 (en) 1997-12-23
KR100460581B1 (en) 2005-04-14
CN1153765C (en) 2004-06-16
PL192353B1 (en) 2006-10-31
NO310144B1 (en) 2001-05-28
UA62914C2 (en) 2004-01-15
DE69623631D1 (en) 2002-10-17
JPH11506118A (en) 1999-06-02
KR19990028431A (en) 1999-04-15
IL122159A (en) 2001-06-14
US5981754A (en) 1999-11-09
PL324216A1 (en) 1998-05-11
CA2225746A1 (en) 1997-01-16
HUP9900055A3 (en) 1999-11-29
HK1014952A1 (en) 1999-10-08
NZ312723A (en) 1999-10-28
AU715090B2 (en) 2000-01-13
CN1189154A (en) 1998-07-29
CA2225746C (en) 2004-05-18
FR2736053A1 (en) 1997-01-03
HUP9900055A2 (en) 1999-04-28
SK283707B6 (en) 2003-12-02
CZ422297A3 (en) 1998-04-15
RU2163237C2 (en) 2001-02-20
JP3302351B2 (en) 2002-07-15
ZA965527B (en) 1997-01-24
IS4641A (en) 1997-12-23
WO1997001536A1 (en) 1997-01-16
JP3147906B2 (en) 2001-03-19
DK0837848T3 (en) 2003-01-06
CY2312B1 (en) 2003-11-14
MX9710472A (en) 1998-03-31
EP0837848B1 (en) 2002-09-11

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